1 Child Term
Identifier | Name | Description |
---|---|---|
DOID:0080260 | autosomal recessive spinocerebellar ataxia 26 | An autosomal recessive cerebellar ataxia that has_material_basis_in compound heterozygous mutation in the XRCC1 gene on chromosome 19q13. |
1 Parent Term
Identifier | Name | Description |
---|---|---|
DOID:936 | brain disease | A central nervous system disease that is located_in the brain. |